Variant #0000726046 (NC_000016.9:g.8895717T>C, NM_000303.2:c.128T>C (PMM2))

Chromosome 16
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.8895717T>C
DNA change (hg38) -
Published as PMM2(NM_000303.2):c.128T>C (p.V43A)
ISCN -
DB-ID PMM2_000080
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PMM2 NM_000303.2 ?/. - c.128T>C r.(?) p.(Val43Ala)
TMEM186 NM_015421.3 ?/. - c.-4246A>G r.(?) p.(=)


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